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Symbol
Name
ID

Myh11
myosin, heavy polypeptide 11, smooth muscle
MGI:102643

Phenotype annotations related to mortality/aging

Darker colors indicate more annotations

Human Phenotypes	Death in infancy	Sudden death
Disease(s) Associated with MYH11	Death in infancy	Sudden death
megacystis-microcolon-intestinal hypoperistalsis syndrome
thoracic aortic aneurysm

Mouse Phenotypes		premature death	neonatal lethality, incomplete penetrance	postnatal lethality, complete penetrance	postnatal lethality, incomplete penetrance
Availability	Mouse Genotype	premature death	neonatal lethality, incomplete penetrance	postnatal lethality, complete penetrance	postnatal lethality, incomplete penetrance
	Myh11^tm1.1Rng/Myh11^tm1.1Rng
	Myh11^tm1Bdr/Myh11^tm1Bdr
	Myh11^tm2Peri/Myh11^tm2Peri

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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